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nsv6424642

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:298,675

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 760 SVs from 63 studies. See in: genome view    
    Submitted genomic21,276,100-21,574,774Question Mark
    Overlapping variant regions from other studies: 766 SVs from 64 studies. See in: genome view    
    Remapped(Score: Perfect):21,276,099-21,574,773Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6424642Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr921,276,10021,574,774
    nsv6424642RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr921,276,09921,574,773

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18230335duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18230335Submitted genomicNC_000009.12:g.212
    76100_21574774dup
    GRCh38 (hg38)NC_000009.12Chr921,276,10021,574,774
    nssv18230335RemappedPerfectNC_000009.11:g.212
    76099_21574773dup
    GRCh37.p13First PassNC_000009.11Chr921,276,09921,574,773

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv18230335<0.001139290
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